Development of a Duplex PCR-NALFIA Assay for the Simultaneous Detection of <i>Macrophomina phaseolina</i> and <i>Verticillium dahliae</i> Causal Agents of Crown and Root Rot of Strawberry

Strawberry crown and root rot diseases are caused by soil-borne pathogens including <i>Macrophomina phaseolina</i> (<i>Mp</i>) and <i>Verticillium dahliae</i> (<i>Vd</i>). The symptoms caused by these pathogens are very similar and difficult to disting...

Full description

Saved in:
Bibliographic Details
Main Authors: Viola Papini, Angelo Meloni, Susanna Pecchia
Format: Article
Language:English
Published: MDPI AG 2025-01-01
Series:Agriculture
Subjects:
Online Access:https://www.mdpi.com/2077-0472/15/2/160
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Strawberry crown and root rot diseases are caused by soil-borne pathogens including <i>Macrophomina phaseolina</i> (<i>Mp</i>) and <i>Verticillium dahliae</i> (<i>Vd</i>). The symptoms caused by these pathogens are very similar and difficult to distinguish, and traditional culture-based detection methods are laborious, time-consuming, and slow in providing results. In this work, we developed a duplex PCR-NALFIA assay using two pairs of species-specific primers labeled at the 5′ end with different molecules for the simultaneous identification of <i>Mp</i> and <i>Vd</i>. For the NALFIA assay, a lateral flow device (LFD) for the detection of two analytes was used. The method was developed by single and duplex PCR (<i>Mp</i>, <i>Vd</i>, <i>Mp</i> + <i>Vd</i>) using increasingly complex biological systems: (i) DNA from pure cultures of the pathogens; (ii) DNA from artificially inoculated cut melon stems; and (iii) DNA from artificially inoculated strawberry plants cv. Aromas. The duplex PCR protocol was effective in detecting the two pathogens within melon tissues and provided good results with strawberry crown tissues only when the DNA samples were purified by removing the PCR inhibitors. The amplicons were used for both agarose gel electrophoresis (AGE) and NALFIA assays and demonstrated the greater sensitivity of the NALFIA assay (10 pg) for simultaneous detection of the two pathogens.
ISSN:2077-0472